A RARE FORM OF MYOCARDIAL INFLAMMATION – COMPLICATIONS WITH A VENTRICULAR ASSIST DEVICE AND SUCCESSFUL TRANSPLANTATION

  • Marcin Schulz Department of Cardiology and Electrotherapy, Silesian Center for Heart Diseases, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland https://orcid.org/0009-0006-4466-5794
  • Rafał Skowronek Department of Pathology, Silesian Center for Heart Diseases, Zabrze, Poland https://orcid.org/0000-0002-1445-3807
  • Alexander Suchodolski Department of Cardiology and Electrotherapy, Silesian Center for Heart Diseases, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland https://orcid.org/0000-0002-5006-7700
  • Jerzy Nożyński Department of Pathology, Silesian Center for Heart Diseases, Zabrze, Poland https://orcid.org/0000-0002-7707-912X
  • Mariola Szulik Department of Cardiology and Electrotherapy, Silesian Center for Heart Diseases, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland; Department of Medical and Health Sciences, WSB University Faculty of Applied Sciences, Dąbrowa Górnicza, Poland https://orcid.org/0000-0002-8229-7279
Keywords: Giant Cell Myocarditis, Post-Inflammatory Cardiomyopathy, Heart Transplantation, Left Ventricular Assist Device, Cardiac Resynchronization Therapy, Endomyocardial Biopsy

Abstract

Giant cell myocarditis (GCM) is a rare, often fulminant inflammatory cardiomyopathy associated with rapid progression to advanced heart failure and high mortality. We report the case of a 52-year-old male with previously undiagnosed GCM who developed post-inflammatory cardiomyopathy leading to severe left ventricular dysfunction. Despite implantation of a cardiac resynchronization therapy defibrillator (CRT-D) and later a HeartMate III left ventricular assist device (LVAD) as a bridge to transplantation, the patient’s condition gradually worsened. Orthotopic heart transplantation was performed 5.5 years after diagnosis, with histopathological analysis of the explanted heart confirming GCM. Post-transplant follow-up over 16 months demonstrated preserved graft function, absence of recurrence, and stable clinical status. This case highlights the importance of histopathological evaluation of explanted hearts, the diagnostic challenges of atypical GCM, and the role of LVAD and heart transplantation in ensuring long-term survival.

 

Video 1. Transthoracic echocardiography showing severely impaired left ventricular contractility with a left ventricular ejection fraction. Watch video

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Published
2025-09-29
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How to Cite
Marcin Schulz, Rafał Skowronek, Alexander Suchodolski, Jerzy Nożyński, & Mariola Szulik. (2025). A RARE FORM OF MYOCARDIAL INFLAMMATION – COMPLICATIONS WITH A VENTRICULAR ASSIST DEVICE AND SUCCESSFUL TRANSPLANTATION. International Journal of Innovative Technologies in Social Science, 4(3(47). https://doi.org/10.31435/ijitss.3(47).2025.3937